A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101706



Internal ID21281246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:128009657..128107113hg38UCSC Ensembl
InnerchrX:127143636..127241092hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3897457
hg1997457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110528
Supporting Variants
Samplessample309
Known GenesACTRT1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101706
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer